Vacuum-sealing-type flexible-film primary battery and method of manufacturing the same

ABSTRACT

Provided are a vacuum-sealing-type flexible-film primary battery and a method of manufacturing the same. The primary battery includes a battery assembly comprising a positive electrode plate including a positive electrode collector having a first conductive carbon layer disposed on a surface-treated inner surface of a first pouch and a positive electrode layer disposed on the first conductive carbon layer of the positive electrode collector, a negative electrode plate including a negative electrode collector having a second conductive carbon layer disposed on a surface-treated inner surface of a second pouch and a negative electrode layer disposed on the second conductive carbon layer of the negative electrode collector, and an adhesion/post-injection polymer electrolyte layer interposed between the positive electrode plate and the negative electrode plate, wherein the battery assembly is completely sealed. The flexible-film primary battery may employ the pouch as a collector film to improve flexibility. Also, the flexible-film primary battery may be completely sealed using the pouch to improve a retention period and cell performance. Furthermore, the flexible-film primary battery may be manufactured using a screen printing technique, thereby facilitating a roll-to-roll sequential process.

CROSS-REFERENCE TO RELATED APPLICATION

This application claims priority to and the benefit of Korean PatentApplication Nos. 10-2009-0076886, filed Aug. 19, 2009 and10-2009-0098147 filed Oct. 15, 2009, the disclosure of which areincorporated herein by reference in its entirety.

BACKGROUND

1. Field of the Invention

The present invention relates to a vacuum-sealing-type flexible-filmprimary battery and a method of manufacturing the same, and morespecifically, to a vacuum-sealing-type flexible-film primary battery,which uses a pouch as a collector substrate and employs a non-metalterminal technique, and a method of manufacturing the primary battery.

2. Discussion of Related Art

In recent years, a vast amount of research has been conducted on activeradio frequency identification (RFID) tag technology. It is expectedthat the active RFID tag technology, which has a far-reaching influenceon a wide variety of fields including digital TVs, home networks, andintelligent robots, will be highlighted as the next-generation essentialindustry that will surpass current code division multiple access (CDMA)technology. In other words, unlike a conventional passive technique ofreading information stored in a tag using a reader, the active RFID tagtechnology may not only lead to a remarkable increase in a tagrecognition distance but also enable sensing of information on objectsand environments around a tag. Ultimately, it is expected that theactive RFID tag technology will expand an information flow region fromcommunication between a human being and an object via networking tocommunication between objects.

In order to drive an RFID tag, it is important to secure an internalpower source completely separated from a reader. In this case, theinternal power source may use a power device appropriate for the RFIDtag, which is compact and lightweight and has a long lifespan. Also, atag coverage may be expanded from a pallet level corresponding to a loadtransportation unit to an item level corresponding to each product.Considering that an applied tag is discarded after its original objectis achieved, it would be most appropriate to apply a primary battery tothe tag. Up to now, a film-type primary battery has partially beenapplied to an RFID tag and recognized as a useful power device.

Meanwhile, more attention has lately been paid to flexible devices.Flexible ubiquitous terminals, such as scroll-type displays, e-papers,flexible liquid crystal displays (LCDs), flexible organic light emittingdiodes (OLEDs), and wearable personal computers (PCs), have lately beenput to practical use, so that the demand for flexible power devices hasnow begun to intensify.

Even if flexible power devices are repeatedly bent, the flexible powerdevices should be free from any cracks in an electrode plate, separationbetween an electrode and an electrolyte, or separation between acollector and the electrode. Thus, to ductilize the collector, thecollector should be formed of a material which is capable of improvingthe ductility of the collector, rather than a metal. Also, the electrodeplate should be easily formed on the ductilized collector, and acompleted battery should be structurally stable to effectively resist tobending or folding. Moreover, manufacture of flexible power devicesshould be simple using equipment that facilitates performing sequentialprocesses.

A conventional film-type primary battery is a film-type 1.5V manganese(Mn) battery in which an electrode and an electrolyte have the sameconfiguration as a typical dry battery and a container formed of apolyethylene terephthalate (PET) package material is used instead of acylindrical can and laminated as a film type. However, although mostpolymer films may drop transmittance of moisture in a gas or air to apredetermined level or lower, it is impossible to completely cut off thetransmittance of moisture in the gas or air. In the long run, this mayresult in leakage or dryness of the electrolyte contained in a cell. Inaddition, since most polymer films, except a polyolefin film, have lowcorrosion resistances to strong acids or strong bases, a direct contactof the polymer films with the electrolyte over a long period may lead tocorrosion of the polymer films. These problems may detrimentally affectthe durability, retention periods, and lifespans of film-type batteries,thereby greatly reducing the performances thereof.

Furthermore, as the function of tags evolves from a battery sustainingfunction into a sensor function, a sensor may be mounted on a tag sothat a driving voltage of the tag may be increased to 3V. Thus, whenconventional 1.5V film-type primary batteries are mounted on a tag, the1.5V film-type primary batteries should be necessarily connected inseries so that the volume of the batteries can be doubled in a limitedspace, thus reducing an energy density.

Meanwhile, in the field of lithium secondary batteries, a pouch formedof a sealed packing material has been proposed to increase a durability,a retention period and a lifespan. A typical pouch has a triplecomposite structure, which includes an outer layer formed of anylon-based polymer film, an inner layer formed of a polypropylene (PP)polymer film, and an intermediate layer formed of aluminum (Al) foilinserted therebetween. Thus, the pouch may have high flexibility andsuch an appropriate mechanical strength as to maintain a predeterminedshape. The inner layer of the pouch, which is formed of PP, may behighly corrosion-resistive to strong acids or strong bases, insoluble inany solvent, and melt only with heat. The intermediate layer formed ofAl foil may function as a perfect barrier layer. Thus, a typical pouchused for a lithium secondary battery may serve as a sealed packingmaterial in a final battery manufacturing process.

By use of the pouch having perfect gas/liquid blocking characteristicsand good vacuum sealing and thermal fusion characteristics, a film-typebattery with good durability and performance may be manufactured using asimple process. To do this, a conductive carbon layer should be directlycoated on the surface of the pouch. Since the PP inner layer of thepouch has a low surface energy and a hydrophobic characteristic, the PPinner layer have a poor wettability in an organic solvent and have apoor coating characteristic, so that it is impossible to directly coatthe conductive carbon layer on the PP inner layer. This is because thecoated conductive carbon layer may be easily delaminated after a dryingprocess and further delaminated when impregnated with an electrolyte.This is due to the fact that the PP inner layer of the pouch is neithercompatible nor miscible with any polar polymer that is currently knownas a binder of an electrode slurry.

A polymer electrolyte used for manufacture of a film-type battery shouldhave good long-term stability because the polymer electrolyte requires along lifespan of at least two years. In other words, components of thepolymer electrolyte should be neither dried nor hardened for at leasttwo years if possible to prevent sudden performance degradation.

Unlike in a conventional method in which electrode plates are laminatedand wound to fabricate a cell, a film-type battery is manufactured bysimply laminating positive and negative plates between which anelectrolyte layer is inserted, thus causing separation or bad contactbetween the electrode plate and the electrolyte layer.

Furthermore, a thin film-type battery needs to be manufactured using asimple low-cost process because of its own properties. However,conventional manufacture of primary and secondary batteries may involvewelding a metal terminal to an electrode plate, which is coated on metalfoil, using ultrasonic waves and vacuum-packing a laminated cellcomponent including an electrolyte. Accordingly, when the conventionalmanufacture of batteries is applied to the thin film-type battery, it isdifficult to overcome high process costs due to a multi-stagemanufacturing process and reduce the unit cost of production of thefilm-type batteries.

SUMMARY OF THE INVENTION

The present invention is directed to a flexible-film primary battery inwhich a pouch formed of a polymer-metal composite film, which completelycuts off transmission of external gases and moisture and has highcorrosion resistance to an electrolyte, is surface-treated and used as apacking material and a collector in order to overcome corrosion of apolymer film, evaporation of the electrolyte due to an open cellstructure, and degradation of retention period and cell performance.

Also, the present invention is directed to a method of manufacturing theabove-described flexible-film primary battery.

One aspect of the present invention provides a flexible-film primarybattery including a battery assembly comprising: a positive electrodeplate including a positive electrode collector having a first conductivecarbon layer disposed on a surface-treated inner surface of a firstpouch and a positive electrode layer disposed on the first conductivecarbon layer of the positive electrode collector; a negative electrodeplate including a negative electrode collector having a secondconductive carbon layer disposed on a surface-treated inner surface of asecond pouch and a negative electrode layer disposed on the secondconductive carbon layer of the negative electrode collector; and anadhesion/post-injection polymer electrolyte layer interposed between thepositive electrode plate and the negative electrode plate., wherein thebattery assembly is completely sealed.

Each of the pouches may be a metal/polymer composite layer including anouter layer, an intermediate layer, and an inner layer that have both avacuum sealing characteristic and a thermal fusion characteristic. Theouter layers of each of the pouches may be a polymer film formed to athickness of about 5 to 50 mm using one selected from the groupconsisting of polyethylene terephthalate (PET), polybutyleneterephthalate (PBT), nylon, high-density polyethylene (HDPE), orientedpolypropylene (o-PP), polyvinyl chloride (PVC), polyimide (PI),polysulfone (PSU), and a combination thereof. The intermediate layers ofeach of the pouches may be a metal layer formed to a thickness of about5 to 50 mm using one selected from the group consisting of aluminum(Al), copper (Cu), stainless steel (SUS), and an alloy thereof. Theinner layers of each of the pouches may be a polymer film formed to athickness of about 5 to 50 mm using one selected from the groupconsisting of cast polypropylene (c-PP), polyethylene (PE), ethylenevinylacetate (EVA), and a combination thereof.

The inner surfaces of each of the pouches may be surface-treated inorder to overcome low surface energy and hydrophobic characteristics tofacilitate formation of a subsequent layer. The surface-treatment may bea hydrophilic surface treatment selected from the group consisting of acorona discharge treatment using plasma, a flaming process, formation ofa silicate (SiO₂) layer, and formation of an oxide coating layer.

Each of the conductive carbon layers may be formed of a conductivecarbon and a polymer binder. The conductive carbon may be one selectedfrom the group consisting of graphite, carbon black, acetylene black,and ketjen black. The polymer binder may be one selected from the groupconsisting of polyvinylidene fluoride (PVDF), a vinylidenefluoride-hexafluoropropylene (HFP) copolymer, polyvinyl chloride (PVC),cellulose, ethylcellulose, carboxymethylcellulose (CMC), polyethylene(PE), polypropylene (PP), ethylvinyl acetate (EVA), and polyvinylalcohol.

The positive electrode layer may include: a positive electrode activematerial selected from manganese dioxide (MnO₂) and vanadium oxide; aconductive material selected from the group consisting of graphite,super-P, carbon black, acetylene black, denka black, ketjen black, andLonza carbon; and a binder selected from the group consisting of PVDF,vinylidene fluoride-HFP copolymer, PVC, polyvinyl alcohol, polyvinylacetate, EVA, CMC, and a mixture of styrene, butadiene rubber andcarboxymethylcellulose.

The negative electrode layer may include lithium foil. Alternatively,the negative electrode layer may include: a negative electrode activematerial formed of zinc (Zn); a conductive material selected from thegroup consisting of graphite, super-P, carbon black, acetylene black,denka black, ketjen black, and Lonza carbon and a binder selected fromthe group consisting of PVDF, a vinylidene fluoride-HFP copolymer, PVC,polyvinyl alcohol, polyvinyl acetate, EVA, CMC, and a mixture ofstyrene, butadiene rubber and carboxymethylcellulose.

The adhesion/post-injection polymer electrolyte layer is a triplecomposite film, which includes a porous polymer matrix; and polymerlayers coated on both sides of the porous polymer matrix and configuredto become adhesive when impregnated with an electrolyte. The porouspolymer matrix may be one selected from the group consisting of linerpaper, nonwoven, a cellophane film, and a combination thereof.Alternatively, the porous polymer matrix may be one selected from thegroup consisting of PVC derivatives, polyacrylonitrile derivatives,polyacrylic acid, cellulose, ethylcellulose, carboxymethylcellulose, anda combination of at least two thereof.

The polymer layer coated on both sides of the porous polymer matrix maybe formed of one selected from the group consisting of polyacrylic acid,cellulose, carboxymethylcellulose, polyvinyl alcohol, and a combinationthereof. Alternatively, the polymer layer coated on both sides of theporous polymer matrix may be formed of one selected from the groupconsisting of PVDF, a vinylidene fluoride-HFP copolymer, PVC,polyvinylidene chloride (PVDC), polyvinyl acetate,poly(methylmethacrylate) (PMMA), and a combination thereof.

The electrolyte may be an aqueous electrolyte or an organic electrolyte.The aqueous electrolyte may be formed of an ammonium chloride saltsolution, a zinc chloride salt solution, or a potassium hydroxide saltsolution, which is dissolved in distilled water. The organic electrolytemay be formed of a lithium salt dissolved in an organic solvent.

Another aspect of the present invention provides a method ofmanufacturing a flexible-film primary battery. The method includesforming a first conductive carbon layer on a surface treated innersurface of a first pouch film to form a positive electrode collector,and forming a positive electrode layer on the conductive carbon layer toform a positive electrode plate; forming a second conductive carbonlayer on a surface treated inner surface of a second pouch film to forma negative electrode collector, and forming a negative electrode layeron the conductive carbon layer to form a negative electrode plate;inserting an adhesion/post-injection polymer electrolyte layer betweenthe positive electrode plate and the negative electrode plate tomanufacture a battery assembly; injecting an electrolyte into thepolymer electrolyte layer of the battery assembly ; and completelysealing the battery assembly to form the flexible-film primary battery.

Each of the pouch films constituting the positive and negative electrodecollectors may have a portion that extends from one side of each of thepouch films and serves as a terminal. Each of the conductive carbonlayers may be formed even on the portion serving as the terminal

The inner surfaces of each of the pouch films may be treated using ahydrophilic surface treatment. The hydrophilic surface treatment may beperformed using a corona discharge treatment using plasma, a flamingprocess, formation of a SiO2 layer, or formation of an oxide coatinglayer.

The conductive carbon layers, the positive electrode layer, and thenegative electrode layer maybe formed using a screen printing process.

BRIEF DESCRIPTION OF THE DRAWINGS

The above and other features and advantages of the present inventionwill become more apparent to those of ordinary skill in the art bydescribing in detail exemplary embodiments thereof with reference to theattached drawings in which:

FIGS. 1A through 1D are plan views of a film primary battery accordingto an exemplary embodiment of the present invention;

FIG. 2 is a cross-sectional view of the film primary battery of FIG. 1D;

FIG. 3 is a flowchart illustrating a method of manufacturing a filmprimary battery according to an exemplary embodiment of the presentinvention;

FIG. 4 is a graph of a voltage relative to a discharge capacity in a1.5V complete-sealing-type film primary battery according to anexemplary Embodiment 1 of the present invention and a primary batteryaccording to Comparative example 1;

FIG. 5 is a graph of a voltage relative to a discharge capacity in a 3Vcomplete-sealing-type film primary battery according to anotherexemplary Embodiment 2 of the present invention and a primary batteryaccording to Comparative example 2; and

FIG. 6 is a graph showing comparison of retention periods of filmprimary batteries according to the exemplary Embodiments 1 & 2 andComparative example 1.

DETAILED DESCRIPTION OF EMBODIMENTS

The present invention will be described more fully hereinafter withreference to the accompanying drawings, in which exemplary embodimentsof the invention are shown.

FIGS. 1A through 1D are plan views of a flexible-film primary batteryaccording to an exemplary embodiment of the present invention, and FIG.2 is a cross-sectional view of the flexible-film primary battery of FIG.1D.

Referring to FIGS. 1A through 1D, the flexible-film primary batteryaccording to the exemplary embodiment of the present invention may havea pouch cell structure having four sides sealed under a vacuum conditionusing a thermal fusion technique. FIG. 1A is a plan view of a positiveelectrode plate 100 including a positive electrode collector having aconductive carbon layer 120 disposed on a surface-treated inner surfaceof a pouch 110 and a positive electrode layer 130 disposed on theconductive carbon layer 120. FIG. 1B is a plan view of anadhesion/post-injection polymer electrolyte layer 200. FIG. 1C is a planview of a negative electrode plate 300 including a negative electrodecollector having a conductive carbon layer 320 disposed on asurface-treated inner surface of a pouch 310 and a negative electrodelayer 330 disposed on the conductive carbon layer 320.

FIG. 1D is a plan view of a flexible-film primary battery in which thepositive electrode plate 100 of FIG. 1A is disposed opposite thenegative electrode plate 300 of FIG. 1B and the polymer electrolytelayer 200 is inserted between the positive electrode plate 100 and thenegative electrode plate 300.

Thus, as shown in FIG. 2, which is a cross-sectional view of theflexible-film primary battery of FIG. 1D, the pouch 310, the conductivecarbon layer 320, the negative electrode layer 330, theadhesion/post-injection polymer electrolyte layer 200, the positiveelectrode layer 130, the conductive carbon layer 120, and the pouch 110may be sequentially laminated.

Each of the pouches 110 and 310 may include a metal/polymer compositelayer including an outer layer, an intermediate layer, and an innerlayer that have both vacuum sealing characteristics and thermal fusioncharacteristics.

More specifically, the outer layers of each of the pouches 110 and 310may be polymer films formed to a thickness of about 5 to 50 mm using oneselected from the group consisting of polyethylene terephthalate (PET),polybutylene terephthalate (PBT), nylone, high-density polyethylene(HDPE), oriented polypropylene (o-PP), polyvinyl chloride (PVC),polyimide (PI), polysulfone (PSU), and a combination thereof. Theintermediate layers of each of the pouches 110 and 310 may be metallayers formed to a thickness of about 5 to 50 mm using one selected fromthe group consisting of aluminum (Al), copper (Cu), stainless steel(SUS), and an alloy thereof. Also, the inner layers of each of thepouches 110 and 310 may be polymer films formed to a thickness of about5 to 50 mm using one selected from the group consisting of castpolypropylene (c-PP), polyethylene (PE), ethylene vinylacetate (EVA),and a combination thereof.

Since the inner surfaces of the pouches 110 and 310 have low surfaceenergy and hydrophobic characteristics, the inner surfaces of thepouches 110 and 310 should be necessarily surface-treated to improvecoating characteristics. In this case, the inner surfaces of the pouches110 and 310 may be treated using a hydrophilic surface treatment. Forexample, the coating characteristics of the inner surfaces of thepouches 110 and 310 may be improved using various micro roughnesstechniques, such as a corona discharge treatment using plasma, a flamingprocess, formation of a silicate (SiO₂) layer, or formation of an oxidecoating layer. As a result, the surface energy of the inner surfaces ofthe pouches 110 and 310 may be improved to about 60 dyne/cm(mN/m) orhigher in case of measurements using test ink.

In the film-type lithium primary battery according to the exemplaryembodiment of the present invention, the pouches 110 and 310 having theinner surfaces coated with the conductive carbon layers 120 and 320 mayconstitute the positive and negative collectors, respectively. Each ofthe conductive carbon layers 120 and 320 may include a conductive carbonand a polymer binder. The conductive carbon may be one selected from thegroup consisting of graphite, carbon black, acetylene black, and ketjenblack. The polymer binder may be one selected from the group consistingof polyvinylidene fluoride (PVDF), a vinylidene fluoride-HFP copolymer,PVC, cellulose, ethylcellulose, carboxymethylcellulose, PE, PP, EVA, andpolyvinyl alcohol.

Here, a ratio of the conductive carbon to the polymer binder may bewithin a range that is typically applicable in the art. For example, aweight ratio of the conductive carbon to the polymer binder may rangefrom about 5:5 to 9.9:0.1.

In the positive electrode collector, the pouch 110 may have a thicknessof about 50 to 180 μm, and the conductive carbon layer 120 may have athickness of about 1 to 30 μm. The pouch 310 and the conductive carbonlayer 320 of the negative electrode collector may have the samethickness ranges as the pouch 110 and the conductive carbon layer 120 ofthe positive electrode collector, respectively. When each of the pouches110 and 310 has a smaller thickness than about 50 μm, each of thepouches 110 and 310 may have a poor vacuum sealing characteristic, whilewhen each of the pouches 110 and 310 has a greater thickness than about180 μm, each of the pouches 110 and 310 may have a poor flexible filmcharacteristic. Also, when each of the conductive carbon layers 120 and320 has a smaller thickness than about 1 μm, the resistance of each ofthe conductive carbon layers 120 and 320 may increase, while when eachof the conductive carbon layers 120 and 320 has a greater thickness thanabout 30 μm, each of the conductive carbon layers 120 and 320 may beinflexible.

The positive and negative electrode collectors may have positive andnegative electrode terminals 140 and 340, respectively. The positive andnegative electrode terminals 140 and 340 may not be tabbed but maycorrespond to non-metallic terminals obtained by extending the pouches110 and 310 in terminal types and coating extensions of the pouches 110and 310 with the conductive carbon layers 120 and 320, respectively.

Meanwhile, since the positive and negative electrode terminals 140 and340 extend from the pouches 110 and 310 and are coated with theconductive carbon layers 120 and 320, respectively, portions of thepouches 110 and 310 on which the conductive carbon layers 120 and 320are formed may be incompletely sealed during a subsequent thermal fusionprocess for completely sealing the flexible-film primary battery.Accordingly, hot melting films 150 and 350 may be further placed on orfused into the portions of the pouches 110 and 310, respectively,thereby enhancing a vacuum sealing state. The hot melting films 150 and350 may be formed of EVA.

The positive electrode layer 130 may be formed by coating the conductivecarbon layer 120 of the positive electrode collector with a positiveelectrode material including a positive electrode active material, aconductive material, and a binder. Specifically, the positive electrodeactive material may be selected from manganese dioxide (MnO₂) andvanadium oxide. Here, the oxide may have a grain size of about 10 to 100μm. The conductive material of the positive electrode material may beone selected from the group consisting of graphite, super-P, carbonblack, acetylene black, denka black, ketjen black, and Lonza carbon. Thebinder of the positive electrode material may be one selected from thegroup consisting of PVDF, a vinylidene fluoride-HFP copolymer, PVC,polyvinyl alcohol, polyvinyl acetate, ethylvinyl acetate,carboxymethylcellulose, and a mixture of styrene butadiene rubber (SBR)and carboxymethylcellulose. A ratio of the positive electrode activematerial, the conductive material, and the binder that constitute thepositive electrode layer 130 may be within a range that is typicallyapplicable in the art. For example, a weight ratio of the positiveelectrode active material, the conductive material, and the binder mayrange from 7:1.5:1.5 to 9.8:0.1:0.1.

The positive electrode layer 130, which is formed on only one side ofthe positive electrode collector to constitute a one-side positiveelectrode plate 100, may have a thickness of about 30 to 150 μm. Whenthe positive electrode layer 130 has a smaller thickness than about 30μm, the capacity and energy density of the primary battery may beexcessively reduced, while when the positive electrode layer 130 has agreater thickness than about 150 on, the positive electrode layer 130may be inflexible.

When the primary battery is a 3V cell, the negative electrode layer 330formed on the conductive carbon layer 320 of the negative electrodecollector may be lithium (Li) foil, which is simply compressed andbonded onto the conductive carbon layer 320. When the primary battery isa 1.5V cell, the negative electrode layer 330 may be formed by coatingthe conductive carbon layer 320 with a negative electrode materialincluding a negative electrode active material, a conductive material,and a binder. Specifically, the negative electrode active material maybe zinc (Zn), and the conductive material of the negative electrodematerial may be one selected from the group consisting of graphite,super-P, carbon black, acetylene black, denka black, ketjen black, andLonza carbon. The binder of the negative electrode material may be oneselected from the group consisting of PVDF, a vinylidene fluoride-HFPcopolymer, PVC, polyvinyl alcohol, polyvinyl acetate, ethylvinylacetate, carboxymethylcellulose, and a mixture of styrene, butadienerubber and carboxymethylcellulose. A ratio of the negative electrodeactive material, the conductive material, and the binder may be within arange that is typically applicable in the art. For example, a weightratio of the negative electrode active material, the conductivematerial, and the binder may range from 7:1.5:1.5 to 9.8:0.1:0.1.

The negative electrode layer 330, which is formed on only one side ofthe negative electrode collector to constitute a one-side negativeelectrode plate 300, may have a thickness of about 15 to 150 μm. Whenthe negative electrode layer 330 has a smaller thickness than about 15μm, the capacity and energy density of the primary battery may beexcessively reduced, while when the negative electrode layer 330 has agreater thickness than about 150 μm, the negative electrode layer 330may be inflexible.

The adhesion/post-injection polymer electrolyte layer 200 of FIG. 1B maybe inserted between the positive electrode plate 100 of FIG. 1A and thenegative electrode plate 300 of FIG. 1C. The adhesion/post-injectionpolymer electrolyte layer 200 may be a triple composite film, which mayinclude a porous polymer matrix and polymer layers, which are coated onboth sides of the porous polymer matrix and configured to becomeadhesive when impregnated with an electrolyte. The porous polymermatrix, which has high mechanical strength and a porous structure, mayfacilitate rapid impregnation of the electrolyte. Also, the polymerlayers coated on both sides of the porous polymer matrix may turnviscous during the impregnation of the electrolyte to coat polymers thatbecome more adhesive to electrodes. Although the polymer electrolytelayer 200 is a multiple film having no adhesive property before theelectrolyte is impregnated, when the polymer electrolyte layer 200 isimpregnated with the electrolyte, the electrolyte may penetrate so thatthe electrolyte is penetrated into pores of the intermediate film, andboth the films may be impregnated with the electrolyte, swell, becomestructurally flexible, and turn into adhesive layers. In this case, theelectrolyte may uniformly spread into an electrolyte region so that theelectrolyte region may be activated into a polymer electrolyte ionconductor.

The porous polymer matrix may be one selected from the group consistingof liner paper, a nonwoven, a cellophane film, and a combinationthereof. In this case, the polymer layers coated on both sides of theporous polymer matrix may be formed of one selected from the groupconsisting of polyacrylic acid, cellulose, carboxymethylcellulose,polyvinyl alcohol, and a combination thereof.

Also, the porous polymer matrix may be formed of a flame-resistantmaterial having a self-extinguishing function to quickly break a contactof a combustible with oxygen during combustion. For example, the porouspolymer matrix may be formed of PVC derivatives, polyacrylonitrilederivatives, polyacrylic acid, cellulose, ethylcellulose,carboxymethylcellulose, or a mixture or copolymer formed of acombination of at least two thereof. For example, the PVC derivativesmay be PVC, PVDC, and so on, and the polyacrylonitrile derivatives maybe one selected from the group consisting of polyacrylonitrile,polymethacrylonitrile, an acrylonitrile-methylmethacrylate copolymer,and a methacrylonitrile-methylmethacrylate copolymer. In this case, thepolymer layers coated on both sides of the porous polymer matrix may beformed of one selected from the group consisting of PVDF, a vinylidenefluoride-HFP copolymer, PVC, polyvinylidene chloride (PVDC), polyvinylacetate (PVA), poly(methylmethacrylate) (PMMA), and a combinationthereof.

The electrolyte, which is injected after the bonding of the polymerelectrolyte layer 200, may be formed of an aqueous electrolyte or anorganic electrolyte. The aqueous electrolyte may be prepared bydissolving an ammonium chloride salt, a zinc chloride salt, or apotassium hydroxide salt in distilled water, or an organic electrolytemay be prepared by dissolving a lithium salt in an organic solvent. Thelithium salt contained in the electrolyte may be one selected from thegroup consisting of lithium perchlorate (LiClO₄), lithium triflate(LiCF₃SO₃), lithium hexafluorophosphate (LiPF₆), lithiumtetrafluoroborate (LiBF₄), lithium trifluoromethane sulfonimide(LiN(CF₃SO₂)₂), and a combination thereof. The organic solvent may beone selected from the group consisting of ethylene carbonate, dimethylcarbonate, diethyl carbonate, ethylmethyl carbonate, dimethyl formamide,tetrahydrofurane, dimethyl acetylamide, n-butyl carbitol,n-methylpyrrolidone, 1,3-dioxolane, dimethylether, diethylether,dimethyl sulfoxide, and a combination thereof.

FIG. 1D is a plan view of the film-type primary battery in which thepositive electrode plate 100 of FIG. 1A and the negative electrode plate300 of FIG. 1C between which the adhesion/post-injection polymerelectrolyte layer 200 of FIG. 1B is inserted are disposed opposite eachother, laminated, and sealed. When the pouches 110 and 310 of thepositive and negative electrode plates 100 and 300 are brought intocontact with each other to allow corners of the pouches 110 and 310 tocorrespond to each other, the coated surfaces of the positive andnegative electrode terminals 140 and 340 are disposed opposite eachother. The positive and negative electrodes terminals 140 and 340 may beformed during formation of the conductive carbon layers 120 and 320 andexposed outside the pouches 110 and 310.

Hereinafter, a method of manufacturing the flexible-film primary batteryof FIG. 1D according to an exemplary embodiment of the present inventionwill be described with reference to FIG. 3.

FIG. 3 is a flowchart illustrating a method of manufacturing aflexible-film primary battery according to an exemplary embodiment ofthe present invention.

Referring to FIG. 3, the method of manufacturing a flexible-film primarybattery according to the exemplary embodiment of the present inventionmay include forming a first conductive carbon layer on a surface-treatedinner surface of a first pouch film to form a positive electrodecollector and forming a positive electrode layer on the first conductivecarbon layer to form a positive electrode plate (step S11); forming asecond conductive carbon layer on a surface-treated inner surface of asecond pouch film to form a negative electrode collector and forming anegative electrode layer on the second conductive carbon layer to form anegative electrode plate (step S12); inserting anadhesion/post-injection polymer electrolyte layer between the positiveelectrode plate and the negative electrode plate to form a batteryassembly in which the negative electrode plate, theadhesion/post-injection polymer electrolyte layer, and the positiveelectrode plate are laminated (step S13); injecting an electrolyte intothe adhesion/post-injection polymer electrolyte layer (step S14); andcompletely sealing the battery assembly to form the primary battery(step S15).

In step S11, before the first conductive carbon layer is formed, thesurface-treated inner surface of the first pouch film may be treatedusing a hydrophilic surface treatment, thereby facilitating theformation of the first conductive carbon layer on the surface-treatedinner surface of the first pouch film.

The hydrophilic surface treatment may be performed using varioustechniques, such as a corona discharge treatment using plasma, a flamingprocess, formation of a silicate (SiO₂) layer, or formation of an oxidecoating layer.

In step S11, the first conductive carbon layer may be coated using ascreen printing process. In this case, the first conductive carbon layermay be coated even on an electrode terminal using a one-time screenprinting process, thereby forming the positive electrode collector.Similarly, the positive electrode layer may be coated on the firstconductive carbon layer using a screen printing process. The positiveelectrode layer may be formed to a thickness of about 30 to 150 μm.

In step S12, as in step S11, the inner surface of the second pouch filmmay be treated using a hydrophilic surface treatment, therebyfacilitating the formation of the second conductive carbon layer on thesurface-treated inner surface of the second pouch film.

In step S12, the second conductive carbon layer may be coated using ascreen printing process. In this case, the second conductive carbonlayer may be coated even on an electrode terminal using a one-timescreen printing process, thereby forming the negative electrodecollector. Similarly, the negative electrode layer may be coated on thesecond conductive carbon layer using a screen printing process. Thenegative electrode layer may be formed to a thickness of about 15 to 150μm.

Although it is exemplarily illustrated that each of the positive andnegative electrode plates is formed using a screen printing process, thepresent invention is not limited thereto. For instance, the conductivecarbon layers and the positive and negative electrode layers may becoated using a slurry coating process of coating a liquid using acoater, a spray coating process of spraying a solution, or an inkjetprinting process using an inkjet head.

In step S13, the facing inner surfaces of the pouch films of the batteryassembly, on which no electrode terminal is formed, may be sealed undera vacuum condition using a thermal fusion process. Specifically, thefacing inner surfaces of the pouch films of the battery assembly, onwhich no electrode terminal is formed, may be fused by applying heat ata temperature of about 100° C. or higher under a reduced pressure.

For example, the polymer electrolyte layer may be a triple compositefilm obtained by dissolving a polymer matrix, which is highly compatiblewith the electrolyte, in a co-solvent, mixing the polymer matrixdissolved in the co-solvent with an inorganic additive, coating bothsides of the porous polymer matrix with the resulting slurry, and dryingthe coated slurry.

Thereafter, in step S14, the electrolyte may be injected into thepolymer electrolyte layer, so that the polymer electrolyte layer may beplasticized, and a portion of the polymer electrolyte layer thatcontacts the electrolyte may become adhesive.

Thereafter, in step S15, the battery assembly may be completely sealed,thereby manufacturing the primary battery. In this case, even thepositive and negative electrode terminals may be sealed under a vacuumcondition using a thermal fusion process, thereby forming acomplete-sealing-type primary battery. In this case, since theconductive carbon layer is formed on the positive and negativeterminals, a sealing state of the primary battery may be weakened.Accordingly, hot melting films may be further placed on or fused intothe positive and negative electrode terminals, respectively, therebyenhancing a vacuum sealing state.

The flexible-film primary battery manufactured using the above-describedprocess may maximize a capacity and energy density in a limited cellspace, have the entire thickness of 1 mm or less, and be capable ofbeing freely bent. Also, a polymer electrolyte layer including anadhesion/post-injection polymer matrix may be used to markedly improvecell safety. Furthermore, the method of the present invention may adopta roll-to-roll process using a conventional screen printing process,thereby facilitating automation, sequential fabrication, and massproduction and reducing manufacturing costs.

Hereinafter, a method of manufacturing a film-type primary batteryaccording to the present invention will be described in further detailwith reference to specific manufacturing examples. However, thefollowing manufacturing examples are provided only for brevity and theinvention should not be construed as limited to the manufacturingexamples set forth therein. Therefore, it will be understood thatvarious changes in form and details may be made in the followingmanufacturing examples without departing from the spirit and scope ofthe present invention.

Embodiment 1: Manufacture of 1.5V Film-Type Manganese (Mn) PrimaryBattery

An inner layer was formed of cast polypropylene (c-PP) to a thickness ofabout 35 mm, an outer layer was formed of nylon to a thickness of about15 mm, and 30 mm-thick aluminum (Al) foil was inserted between the innerand outer layers. The inner layer, the Al foil, and the outer layer werelaminated to form a 75 mm-thick Al pouch. An inner surface of the Alpouch was hydrophilic-treated using a corona discharger in anatmospheric environment until a surface energy reached about 50 dyne/cmor higher. The hydrophilic-treated inner surface of the Al pouch lostits peculiar gloss and became rough. It could be confirmed that whendrops of water fell on the surface-treated inner surface of the Alpouch, they did not stand but spread out to facilitate formation of acoating layer.

Jelly-like highly viscous carbon paste, which was manufactured bydissolving 5% by weight PVDF in N-methyl pyrrolidone (NMP) and adding95% by weight graphite, was coated on the surface-treated inner surfaceof the Al pouch using a screen printer, thereby forming a positiveelectrode collector. After the screen printing process, a driedconductive carbon layer had a thickness of about 20 mm and an area of4.3 cm×4.3 cm. In this case, not only a current collecting area but alsoa lead line with a width of about 0.8 cm and a length of 2.5 cm werecoated with the conductive carbon layer at once. Subsequently, the leadline served as positive and negative electrode terminals aftercompletion of a final cell.

A mixture was obtained by mixing an SBR emulsion with 3% by weightcarboxymethylcellulose (CMC) dissolved in distilled water in a weightratio of 1:1, and then mixed with 90% by weight electrochemicallysynthesized electrolytic manganese oxide (EMD) (functioning as apositive electrode active material), 5% by weight graphite (functioningas a conductive material), and 5% by weight SBR/CMC (functioning as abinder) based on the total weight of the co-solvent, thereby forming aslurry. The slurry was coated on the conductive carbon layer to form aone-side oxide positive electrode plate to a thickness of about 100 μm.

In order to form a negative electrode plate, like the positive electrodeplate, a conductive carbon layer was formed on the inner layer of thepouch to form a negative electrode collector. Thereafter, a mixture wasobtained by mixing an SBR emulsion with 3% by weight CMC dissolved indistilled water in a weight ratio of 1:1, and then mixed with 90% byweight Zn powder having an average diameter of about 75 mm or less(functioning as a negative electrode active material), 5% by weightgraphite (functioning as a conductive material), and 5% by weightSBR/CMC (functioning as a binder) based on the total weight of theco-solvent, thereby forming a slurry. The slurry was coated on theconductive carbon layer to form a one-side negative electrode plate to athickness of about 50 μm.

In order to form an adhesion/post-injection polymer electrolyte layer, apolyacrylic acid was dissolved in distilled water, and 15% by weighthydrophobic silica based on the total weight of a polymer matrix wasadded, and a mixture was coated on a nonwoven to a thickness of about 15mm or more, thereby forming a triple composite layer. Theadhesion/post-injection polymer electrolyte layer having a triplestructure was inserted between the positive and negative electrodeplates, and ends of first through third sides other than a fourth sidehaving the positive and negative electrodes terminals were bonded to oneanother using a thermal fusion process. Afterwards, a 1 mL aqueouselectrolyte obtained by dissolving a 3M ammonium chloride salt indistilled water was injected, and the remaining fourth side having thepositive and negative electrode terminals was fused and bonded under avacuum compressed-bonding condition, thereby completing manufacture of asealing-type film primary battery. In this case, since a sealing stateof portions of the fourth side on which the conductive carbon layerswere formed might weaken during the thermal fusion process, EVA filmswere further placed on the portions of the fourth side on which thecarbon conductive layers were formed.

In this case, 3% by weight potassium dichromate (functioning as adepolarizer) was further added to the aqueous electrolyte. After theelectrolyte was injected, the electrolyte permeated into the nonwovenand both the polymer coating layers so that the electrolyte was remainedin the porous nonwoven, while both the coating layers formed of apolyacrylic acid were impregnated and activated into a highly adhesiveelectrolyte layer and remained in physical contact with the positive andnegative electrode plates.

Embodiment 2: Manufacture of 3V Film-Type Lithium Primary Battery

Positive and negative electrode collectors were formed in the samemanner as in Embodiment 1, and the positive electrode collector wascoated with the same positive electrode active material as in Embodiment1, thereby forming a positive electrode plate. However, to form anegative electrode plate, 50 μm-thick Li foil was cut to an area of 4.3cm×4.3 cm, placed on the negative electrode collector, and bonded to thenegative electrode collector under pressure.

Also, a polymer electrolyte layer was formed in the same manner as inEmbodiment 1 except that a vinylidene fluoride-HFP copolymer wasdissolved in an NMP co-solvent and 25% by weight hydrophobic silicabased on the total weight of a polymer matrix was added, and theresulting solution was coated on both 16 mm-thick PE porous layers to athickness of about 5 mm or more to form a triple composite layer. Inthis case, an electrolyte was injected and activated in the same manneras in Embodiment 1 except that the electrolyte was not an aqueouselectrolyte but a 1M organic electrolyte obtained by dissolving alithium hexafluorophosphate (LiPF₆) salt in a solvent prepared by mixingethylene carbonate and dimethyl carbonante in a weight ratio of 1:1. Asa result, manufacture of a 3V complete-sealing-type film primary batterywas completed.

Comparative Examples

In order to analyze the lifespan, capacity, film thickness, and processsimplicity of the 1.5V film-type primary battery and 3V film-typeprimary battery prepared by Embodiments 1 and 2, respectively, a 1.5Vopen-type film battery and a 3V pouch-type film battery in whichconventional metal collectors were formed using each of Al and nickel(Ni) were manufactured. In this case, the 1.5V open-type film batterywas manufactured under the same conditions except that the same positiveand negative electrode plates as in Embodiment 1 were formed on a PETfilm instead of a pouch and four corners were not vacuum-sealed butsealed using an adhesive tape (Comparative example 1). The 3V pouch-typefilm battery was manufactured under the same conditions except that apouch was used only as a packing material during a final vacuum sealingprocess, positive and negative electrode plates were formed byrespectively coating Al and Cu foils with positive and negativeelectrode layers formed of the same material and processed with Al andNi tabs, respectively, using an ultrasonic welding machine, and a PEisolation layer was used as an electrolyte instead of an adhesiveelectrolyte, and the electrolyte was post-injected before the vacuumsealing process (Comparative example 2).

Comparison between Embodiments 1 and 2 with Comparative Examples 1 and 2

A variation of voltage relative to discharge capacity of the 1.5Vcomplete-sealing-type film primary battery of Embodiment 1 was comparedwith that of Comparative example 1 as shown in FIG. 4.

Referring to FIG. 4, the film-type primary battery of

Embodiment 1 required an initial open-circuit voltage (OCV) of 1.5V andhad a cell capacity of about 4.0 mAh/cm² or more when discharged to 1.0Vunder a current condition of C/10 (1 mA). That is, the film-type primarybattery of Embodiment 1 had about 1.4 times the discharge capacity ofthe 1.5V open-type film primary battery of Comparative example 1, whichhad the same size and thickness as the primary battery of Embodiment 1.

A variation of voltage relative to discharge capacity of the 3Vcomplete-sealing-type film primary battery of Embodiment 2 was comparedwith that of Comparative example 2 as shown in FIG. 5.

Referring to FIG. 5, the film-type primary battery of Embodiment 2required an initial OCV of 3.7V and had a cell capacity of about 5.0mAh/cm2 or more when discharged to 2.0V under a current condition ofC/10 (1 mA). That is, the film-type primary battery of Embodiment 2 hadabout 1.5 times the discharge capacity of the 3V pouch-type primarybattery of Comparative example 2, which had the same size and thicknessas the primary battery of Embodiment 2.

In order to analyze the retention periods of the film-type primarybatteries of Embodiments 1 and 2, a variation of an OCV relative to timeof each of the film-type primary batteries of Embodiments 1 and 2 wasmeasured every month for 2 years and compared with that of Comparativeexample 1 as shown in FIG. 6.

Referring to FIG. 6, the OCV of each of the film-type primary batteriesaccording to Embodiments 1 and 2 of the present invention were reducedby lower than 1% for 2 years. Thus, it can be confirmed that thefilm-type primary batteries of Embodiments 1 and 2 exhibited lowself-discharge rates and good lifespan characteristics.

A flexible-film primary battery according to exemplary embodiments ofthe present invention may employ a pouch as a collector substrate toensure flexibility and cut off transmission of gases and moisture,thereby enabling manufacture of a sealing-type film battery.

Also, a conductive layer and an electrode may be directly coated on asurface-treated pouch so that a cell can be completed during a finaloperation through a one-time roll-to-roll sequential process. Inparticular, inner layers of pouches may freely undergo a thermal fusionprocess in portions other than the electrode and the conductive layer,thereby facilitating manufacture of the film battery.

Furthermore, a flexible-film primary battery according to the presentinvention may employ a triple adhesion/post-injection layer including aporous core film, which is easily impregnated with an electrolyte, andpolymer layers, which are coated on both sides of the porous core filmto be highly adhesive to electrodes, thereby facilitating performingsequential processes.

A flexible-film primary battery may be freely embodied irrespective of a1.5V battery or a 3V battery and employ a collector with a pouch so thata conductive carbon layer may be extended and used as a nonmetalterminal without forming or adding positive and negative metalterminals.

According to the present invention, a flexible-film primary battery canbe simply sealed under a vacuum condition using a thermal fusiontechnique, thereby improving a retention period, a lifespan, and asafety characteristic.

In the drawings and specification, there have been disclosed typicalexemplary embodiments of the invention and, although specific terms areemployed, they are used in a generic and descriptive sense only and notfor purposes of limitation. As for the scope of the invention, it is tobe set forth in the following claims. Therefore, it will be understoodby those of ordinary skill in the art that various changes in form anddetails may be made therein without departing from the spirit and scopeof the present invention as defined by the following claims.

1. A flexible-film primary battery including a battery assemblycomprising: a positive electrode plate including a positive electrodecollector having a first conductive carbon layer disposed on asurface-treated inner surface of a first pouch and a positive electrodelayer disposed on the first conductive carbon layer of the positiveelectrode collector; a negative electrode plate including a negativeelectrode collector having a second conductive carbon layer disposed ona surface-treated inner surface of a second pouch and a negativeelectrode layer disposed on the second conductive carbon layer of thenegative electrode collector; and an adhesion/post-injection polymerelectrolyte layer interposed between the positive electrode plate andthe negative electrode plate, wherein the battery assembly is completelysealed.
 2. The primary battery of claim 1, wherein each of the first andsecond pouches is a metal/polymer composite layer including an outerlayer, an intermediate layer, and an inner layer that have both a vacuumsealing characteristic and a thermal fusion characteristic.
 3. Theprimary battery of claim 2, wherein the outer layers of each of thefirst and second pouches are polymer films formed to a thickness ofabout 5 mm to about 50 mm using one selected from the group consistingof polyethylene terephthalate (PET), polybutylene terephthalate (PBT),nylone, high-density polyethylene (HDPE), oriented polypropylene (o-PP),polyvinyl chloride (PVC), polyimide (PI), polysulfone (PSU), and acombination thereof, the intermediate layers of each of the first andsecond pouches are metal layers formed to a thickness of about 5 mm toabout 50 mm using one selected from the group consisting of aluminum(Al), copper (Cu), stainless steel (SUS), and an alloy thereof, and theinner layers of each of the first and second pouches are polymer filmsformed to a thickness of about 5 mm to about 50 mm using one selectedfrom the group consisting of cast polypropylene (c-PP), polyethylene(PE), ethylene vinylacetate (EVA), and a combination thereof.
 4. Theprimary battery of claim 1, wherein the inner surfaces of each of thefirst and second pouches are treated using a hydrophilic surfacetreatment.
 5. The primary battery of claim 1, wherein each of the firstand second conductive carbon layers is formed of a conductive carbonselected from the group consisting of graphite, carbon black, acetyleneblack, and ketjen black and a polymer binder selected from the groupconsisting of polyvinylidene fluoride (PVDF), a vinylidene fluoride-HFPcopolymer, PVC, cellulose, ethylcellulose, carboxymethylcellulose, PE,PP, EVA, and polyvinyl alcohol.
 6. The primary battery of claim 1,wherein the positive electrode layer comprises: a positive electrodeactive material selected from manganese dioxide (MnO₂) and vanadiumoxide; a conductive material selected from the group consisting ofgraphite, super-P, carbon black, acetylene black, denka black, ketjenblack, and Lonza carbon; and a binder selected from the group consistingof PVDF, a vinylidene fluoride-HFP copolymer, PVC, polyvinyl alcohol,polyvinyl acetate, ethylvinyl acetate, carboxymethylcellulose, and amixture of styrene, butadiene rubber and carboxymethylcellulose.
 7. Theprimary battery of claim 1, wherein the negative electrode layerincludes lithium foil.
 8. The primary battery of claim 1, wherein thenegative electrode layer comprises: a negative electrode active materialformed of zinc (Zn); a conductive material selected from the groupconsisting of graphite, super-P, carbon black, acetylene black, denkablack, ketjen black, and Lonza carbon and a binder selected from thegroup consisting of PVDF, a vinylidene fluoride-HFP copolymer, PVC,polyvinyl alcohol, ethylvinyl acetate, carboxymethylcellulose, and amixture of styrene, butadiene rubber and carboxymethylcellulose.
 9. Theprimary battery of claim 1, wherein the adhesion/post-injection polymerelectrolyte layer is a triple composite film including: a porous polymermatrix; and polymer layers coated on both sides of the porous polymermatrix and configured to become adhesive when impregnated with anelectrolyte.
 10. The primary battery of claim 9, wherein the porouspolymer matrix is selected from the group consisting of liner paper,nonwoven, a cellophane film, and a combination thereof.
 11. The primarybattery of claim 9, wherein the porous polymer matrix is selected fromthe group consisting of PVC derivatives, polyacrylonitrile derivatives,polyacrylic acid, cellulose, ethylcellulose, carboxymethylcellulose, anda combination of at least two thereof.
 12. The primary battery of claim10, wherein the polymer layer coated on both sides of the porous polymermatrix is formed of one selected from the group consisting ofpolyacrylic acid, cellulose, carboxymethylcellulose, polyvinyl alcohol,and a combination thereof.
 13. The primary battery of claim 11, whereinthe polymer layer coated on both sides of the porous polymer matrix isformed of one selected from the group consisting of PVDF, a vinylidenefluoride-PVDF copolymer, PVC, polyvinylidene chloride (PVDC), polyvinylacetate, poly(methylmethacrylate) (PMMA), and a combination thereof. 14.The primary battery of claim 9, wherein the electrolyte is an aqueouselectrolyte formed by dissolving an ammonium chloride salt, a zincchloride salt, or a potassium hydroxide salt in distilled water, or anorganic electrolyte formed by dissolving a lithium salt in an organicsolvent.
 15. A method of manufacturing a flexible-film primary battery,comprising: forming a first conductive carbon layer on a surface-treatedinner surface of a first pouch film to form a positive electrodecollector, and forming a positive electrode layer on the firstconductive carbon layer to form a positive electrode plate; forming asecond conductive carbon layer on a surface-treated inner surface of asecond pouch film to form a negative electrode collector, and forming anegative electrode layer on the second conductive carbon layer to form anegative electrode plate; inserting an adhesion/post-injection polymerelectrolyte layer between the positive electrode plate and the negativeelectrode plate to manufacture a battery assembly; injecting anelectrolyte into the polymer electrolyte layer of the battery assembly;and completely sealing the battery assembly to form a primary battery.16. The method of claim 15, wherein each of the first and second pouchfilms constituting the positive and negative electrode collectors has aportion that extends from one side of each of the first and second pouchfilms and serves as a terminal.
 17. The method of claim 16, wherein eachof the first and second conductive carbon layers is formed even on theportion serving as the terminal.
 18. The method of claim 15, wherein theinner surfaces of each of the first and second pouch films are treatedusing a hydrophilic surface treatment.
 19. The method of claim 18,wherein the hydrophilic surface treatment is performed using oneselected from the group consisting of a corona discharge treatment usingplasma, a flaming process, formation of a silicate (SiO₂) layer, andformation of an oxide coating layer.
 20. The method of claim 15, whereinthe first and second conductive carbon layers, the positive electrodelayer, and the negative electrode layer are formed using a screenprinting process.